8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SURE FLOW TUBING
FDA 510(k)
FDA Class 1
·Anesthesiology
ACUMED
FDA UDI
Acumed LLC·10806378043895·2.3mm Depth Probe
VIGILANCE CCO/CEDV & VIGILANCE CCO/SVO2/CEDV MONITORS
FDA 510(k)
FDA Class 2
·Cardiovascular
RELIEVE LAMINOPLASTY FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PK DISSECTING FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·May 8, 2014
UNKNOWN DEPUY ASR ACETABULAR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·October 22, 2012
CAREASSIST BED
FDA Adverse Event
Malfunction
·HILL-ROM PLUVIGNER·Product code FNL·August 4, 2010
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021